Regulatory Affairs CMC Manager / Snr Manager, work on NBEs (code BE)

Employer
Advanced Regulatory (UK & Europe)
Location
Brussels, Belgium
Salary
Competitive
Closing date
14 Oct 2020

View more

Discipline
Regulatory Affairs, Project Management, Regulatory Project Management
Hours
Full Time
Contract Type
Permanent
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Regulatory Affairs CMC Manager / Snr Manager, work on NBEs

We have a permanent opportunity for a Snr Manager / Manager Regulatory Affairs CMC to join our client on their exciting journey.

Note: My client has committed to do digital hiring using Skype (VC), and has a new digital on-boarding and induction training process in place to allow a smooth transition during MERS-COV-2 outbreak. During the next period, new hires will be allowed to work from home full-time, until such a time occurs when normal working returns.

Do you already have CTA / IMPD experience authoring and delivering Regulatory CMC submission documents and now want to do more first MAA / BLA submissions for novel products?

This Regulatory Affairs CMC role is based in Brussels, Belgium. Our client is an international Biopharmaceutical company with several block busters and a strong pipeline of exciting new biological products coming up in development. This organisation excels as a company because it invests in its people as well as its science, it has being able to foster a culture of innovation, collaboration, creativity and maintain continual high standards.

Responsibilities:

  • You will work in an international environment supporting a new MAA and subsequently moving on to supporting and leading biological molecules in development.
  • Lead projects as assigned and be responsible for the preparation, authoring and compilation of Regulatory CMC dossier for CTAs and MAAs (IMPDs, INDs, Module 3 for MAAs, BLAs etc.).
  • Be responsible for regional regulatory expertise and have an input into the development and implementation of global regulatory CMC strategy.
  • Manager the CMC aspects of regional Health Authority interactions.

Who's right for the job?

You will have 5 plus years relevant industry experience. Most of this would be in the Regulatory Affairs CMC field and you would have successfully authored and contributed to delivering CMC submission documents for biological products in development and marketed products. Direct communication experience with Health Authorities on CMC matters is required. Good level of English is a must as this is the business language in this organization.

In return you will:

  • This is an opportunity to become an integral part of an expanding Regulatory Affairs CMC team (these are new roles) in a successful company
  • Work in the Global HQ where most of the team is based and be supported by experienced Regulatory CMC leadership in a growing organization where the next career step will be open for
  • Earn a competitive for the industry salary, with a bonus and other company benefits. Have the flexibility to work from home 2 days per week.

Interested in the above? I look forward to hearing from you!

Who are we?

ADV Talent is a niche recruitment agency hiring for major bio/pharmaceutical companies and healthcare organizations mainly in the field of Regulatory Affairs and Regulatory CMC. We want individuals to eb self-actualized for their own hiring process. This brings out the individuals to embrace change and identify with their next career move as an opportunity to grow. By this, our applicants grow, and so do our clients.
 

To Apply!

To apply, please send a full CV to Oli@AdvTalent.com, or alternatively, contact Oli or Theo on +44 (0)207 801 3388. We are assigned these roles by our client and will provide you with support throughout the hiring process.
 

About Advanced Search & Our Network

Advanced Search, has a network of affiliated companies including ADV Regulatory, and ADV Talent Partners. Together, we are specialists in Regulatory Affairs and Life Sciences recruitment especially around mAbs and biologicals for roles in R&D and Commercialization and have been established and hiring in this area since 2005.

Our Regulatory Affairs team know their subject matter areas and our mission is to help you grow your career each and every step of the way. We have helped many of today's leading companies develop strong regulatory sciences functions and are known for hiring complimentary teams that work well with each other, at owner-contributor, strategy leading and people management levels.

Contact us today to see how we can help you make that next career move on

+44 (0)207 801 3380

All applications are kept in confidence and we invite applications from all members of the Academic, Research & Development based bio-pharmaceutical community.

Advanced Regulatory is a new recruitment organisation. Our consultants are industry known and highly experienced in Regulatory Affairs recruitment. We have assembled a team with competencies in databased contingency recruitment, Search & Selection as well as Creative & Campaign management. Our specialism is Regulatory Affairs. We know that successful submissions are underpinned not by one but many people, all working in cohesion. Whether you require a new career position or a new recruit at junior, mid or senior level, we would like to assist you. Our remit is to provide Regulatory Affairs professionals at all levels to pharmaceutical, regulatory consulting, biopharmaceutical and clinical research organisations.

Contact Us
  • Suite 8 Penhurst House
  • 352-356 Battersea Park Road
  • SW11 3BY
  • GB
  • +44 (0)20 7801 3380
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